Departments of Pharmaceutical Sciences, University of California, Irvine, California 92697, United States.
Departments of Chemistry, University of California, Irvine, California 92697, United States.
Bioconjug Chem. 2022 Oct 19;33(10):1876-1884. doi: 10.1021/acs.bioconjchem.2c00348. Epub 2022 Sep 27.
Cell-to-cell communications are critical to biological processes ranging from embryonic development to cancer progression. Several imaging strategies have been developed to capture such interactions, but many are challenging to deploy in thick tissues and other complex environments. Here, we report a platform termed Luminescence to Observe and Track Intercellular Interactions (LOTIIS). The approach features split fragments of a luciferase enzyme that reassemble when target cells come into proximity. One fragment is secreted by "sender" cells, and the complementary piece is secreted by "receiver" cells. Split reporter assembly is facilitated by a single chain variable fragment (scFv)-peptide interaction on the receiver cell, resulting in localized light production. We demonstrate that LOTIIS can rapidly label cells in close proximity in a time- and distance-dependent fashion. The platform is also compatible with bioluminescence resonance energy transfer probes for multiplexed imaging. Collectively, these data suggest that LOTIIS will enable a variety of cellular interactions to be tracked in biological settings.
细胞间通讯对于从胚胎发育到癌症进展等生物过程至关重要。已经开发出几种成像策略来捕捉这些相互作用,但许多策略在厚组织和其他复杂环境中难以部署。在这里,我们报告了一种称为发光观察和跟踪细胞间相互作用(LOTIIS)的平台。该方法的特点是将荧光素酶酶的分裂片段重新组装,当靶细胞接近时。一个片段由“发送器”细胞分泌,互补片段由“接收器”细胞分泌。在接收器细胞上,通过单链可变片段(scFv)-肽相互作用促进分裂报告分子的组装,从而产生局部光产生。我们证明 LOTIIS 可以快速标记近距离的细胞,时间和距离依赖性方式。该平台还与用于多重成像的生物发光共振能量转移探针兼容。总的来说,这些数据表明 LOTIIS 将能够在生物环境中跟踪各种细胞相互作用。